Tech Writer Job Description Supporting Pharmaceutical Manufacturing Operations and Technical groups to; *Own document revision and routing on document management system and drive on time approval *Design, update and improve facility/process procedures and business processes. *Design, update and improve Manufacturing Batch Records. *Design, generate and update Operations Area Logbooks *Design, generate and update Training Documentation *Design, update and improve EH&S systems and documentation. *Design and generate PQ Protocols *Design update/improve other documentations associated with the large molecule business. *Managing documents in the site documentation management system in line with the site quality assurance program and local standard operating procedures. Opportunity to: *Support a dynamic Large Molecule manufacturing environment. *Develop/learn key understanding of core manufacturing principles. *Involvement in New Product Introductions (NPI). *Deliver in innovative Manufacturing Areas. *Support multiple manufacturing functions (Eng, Chemistry, QA, EHS, Micro) Requirements: *Relevant engineering/ science 3rd level qualification or operational experience *Masters in engineering / science is desirable *Previous pharma production, operations/ projects/process experience *Strong sense of customer focus and teamwork *Previously demonstrated flexibility and willingness to take on different job tasks *Self-motivated/ proactive approach with the ability to operate without close supervision *Proven ability to deal with unexpected issues using problem solving skills *Commitment to meet deadlines *Right first time attitude. *Demonstrated technical writing skills in the generation of documents and high level of IT skills *Good planning and organisation skills essential Skills: Documentation experience Production experience Pharma Background.